材料科学
硼酚
钼
锂(药物)
硫黄
硼
二硫化钼
化学工程
纳米技术
无机化学
化学
有机化学
冶金
单层
医学
内分泌学
工程类
作者
Rong Wu,Huakai Xu,Yuwei Zhao,Chenyang Zha,Jun Deng,Chengyu Zhang,Gang Lü,Tianshi Qin,Wei Wang,Yao Yin,Chao Zhu,Lin Wang,Gang Ouyang,Wei Huang
标识
DOI:10.1016/j.ensm.2020.07.040
摘要
High-performance lithium-sulfur batteries are limited by the severe “shuttle effect” of polysulfide migration. To entrap and immobilize polysulfides, the development of catalytic material is an effective strategy for improving the lithium-sulfur batteries. Herein, we demonstrate that borophene-like boron subunits-inserted molybdenum frameworks of molybdenum diboride (MoB2) serves as a polysulfide-anchoring center to power redox reaction processing under the high-efficient electron transfer conditions. Specifically, MoB2 not only offers active sites to anchor polysulfide via covalent B-B and metallic Mo-Mo bonds-based low lithiation structure, but also provides a high conductivity to accelerate polysulfide conversion kinetics. With these advances, the liquid Li2S6-based MoB2 electrode (area: 2 cm2) offers a high initial capacity of 1116 mAh/g, and holds 558 mAh/g at 2 C after 500 cycles. Furthermore, the currently proposed MoB2 catalyst may significantly propel the advancement of electrocatalysis technology from lithium-sulfur batteries to metal-air batteries and carbon dioxide/nitrogen electrochemical reduction.
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